US3932623A - Method of treating schizophrenia - Google Patents

Method of treating schizophrenia Download PDF

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Publication number
US3932623A
US3932623A US05/480,546 US48054674A US3932623A US 3932623 A US3932623 A US 3932623A US 48054674 A US48054674 A US 48054674A US 3932623 A US3932623 A US 3932623A
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schizophrenia
trh
treatment
treating schizophrenia
pyro
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US05/480,546
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Ian C. Wilson
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0821Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
    • C07K5/0825Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp and Glp-amino acid; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/04Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/06Tripeptides
    • A61K38/066TRH, thyroliberin, thyrotropin releasing hormone

Definitions

  • the present invention relates to an improved method of treating schizophrenia.
  • Acute toxic phenomena may refer to many physical systems: skin rashes, hepatic and renal dysfunction, blood dyscrasias, and extrapramidal nervous system signs and symptoms have all been documented as complicating these treatments.
  • the present invention provides this method.
  • TRH thyrotropin releasing hormone
  • thyrotropin releasing hormone A neurosecretory product known as "thyrotropin releasing hormone" hereinafter referred to as TRH, is an extremely useful drug and laboratory substance. TRH was previously isolated by multi-step fractionation of hypothalamic extracts. This complex isolation yielded the valuable but expensive product. It has now been established that L-pyroglutamyl-L-histidyl-L-proline amide, a synthetic product, hereinafter referred to as (pyro) glu-his-pro(NH 2 ) exhibits the same chemical and hormonal properties as the porcine TRH (Folkers et al., Biochem. and Biophys. Research Comm. 39; No. 1: 110-113, 1970). See also U.S. Pat. No. 3,737,549. The scientific community now has reached the conclusion that native TRH is chemically L-pyroglutamyl-L-histidyl-L-proline amide.
  • the subjects to be treated with this substance are diagnostically well-defined cases of schizophrenia presenting with classical schizophrenic symptomatology: autistic thinking, thought retardation, thought blocking, hallucinations, delusions, flattened affect, and socially withdrawn behavior.
  • TRH or (pyro) glu-his-pro(NH 2 ) 100-1000 mcg. improvement in all areas of psychopathology occurs.
  • the thought processes become more lucid and realistic with an increase in spontaneity of verbal expression.
  • the subjects themselves remark about the sudden clarity of their thinking. Hallucinatory phenomena disappear and the subjects speak with insight about their previously disturbed perceptions. Concomitant changes in affect occur.
  • TRH or (pyro) glu-his-pro(NH 2 ) particularly useful agents in the treatment of schizophrenia.
  • the active ingredients useful in the practice of this invention can be formulated into various pharmaceutical dosage forms such as tablets, capsules, pills, sterile aqueous or nonaqueous solutions for parenteral injection administration, and the like, for immediate or sustained release, by combining one or more of the active compounds with suitable pharmaceutically acceptable carrier or diluents according to methods, well known in the art.
  • Such dosage forms may additionally include excipients, binders, fillers, flavoring and sweetening agents and other therapeutically inert ingredients necessary in the formulation of the desired pharmaceutical preparation.
  • Tablets containing 400 mcg. TRH and having the following composition are prepared according to methods well known in the art.
  • Ampoules for intravenous use are prepared containing 200 mcg. of (pyro) glu-his-pro(NH 2 ) in 1 ml. of sterile physiologic saline.
  • TRH for purposes of the present invention there may be used not only TRH or (pyro) glu-his-pro(NH 2 ) in the treatment of schizophrenia but also the use of congeners and derivatives thereof is contemplated, and such materials are deemed to be the equivalents of the parent materials. It has been shown that certain congeners of TRH, like the parent substance, antagonize the actions of pentobarbital in mice.

Abstract

An improved method of treating schizophrenia and allied conditions such as childhood schizophrenia and autism using thyrotropin releasing hormone, L-pyroglutamyl-L-histidyl-L-proline amide, or its congeners as a treating agent.

Description

The present invention relates to an improved method of treating schizophrenia.
There are a number of clinically effecitve psychopharmaceutical substances used in the treatment of schizophrenia, mainly phenothiazines, butyrophenones, and thioxanthenes. The major drawback to these medications is their partial effectiveness. These medications are generally directed towards relied of various "target symptoms," resulting in a general beneficial modification of behavior. However, the fundamental pathological personality characteristics of the disease are generally left unchanged. Acute and chronic toxic phenomena are also commonly recorded with these medications. Acute toxic phenomena may refer to many physical systems: skin rashes, hepatic and renal dysfunction, blood dyscrasias, and extrapramidal nervous system signs and symptoms have all been documented as complicating these treatments. Chronic administration of these drugs as is often required in schizophrenia, may result in irreversible toxic effects to the skin, the eyes, the cardiovascular system, and the central nervous system. Other modalities of treatment less frequently used now than formerly are insulin comatherapy and electroschock treatment. The disadvantages of these therapies are of a similar nature to that of the use of psychopharmacological substances. These treatment modalities mainly modify the clinical symptom picture without modifying the basic personality pathology. Inherent in these therapies are certain severe complications which may result in severe physical damage or perhaps death of the subject. Both of these treatments have a substantial mortality rate.
Therefore, there exists a need for an improved method of treatment of schizophrenia. The present invention provides this method.
A neurosecretory product known as "thyrotropin releasing hormone" hereinafter referred to as TRH, is an extremely useful drug and laboratory substance. TRH was previously isolated by multi-step fractionation of hypothalamic extracts. This complex isolation yielded the valuable but expensive product. It has now been established that L-pyroglutamyl-L-histidyl-L-proline amide, a synthetic product, hereinafter referred to as (pyro) glu-his-pro(NH2) exhibits the same chemical and hormonal properties as the porcine TRH (Folkers et al., Biochem. and Biophys. Research Comm. 39; No. 1: 110-113, 1970). See also U.S. Pat. No. 3,737,549. The scientific community now has reached the conclusion that native TRH is chemically L-pyroglutamyl-L-histidyl-L-proline amide.
We have now found that when 100-1000 mcg. TRH or (pyro) glu-his-pro(NH2) is administered to schizophrenics that remarkably beneficial changes occur in these subjects in the spheres of thought, affect and behavior.
The subjects to be treated with this substance are diagnostically well-defined cases of schizophrenia presenting with classical schizophrenic symptomatology: autistic thinking, thought retardation, thought blocking, hallucinations, delusions, flattened affect, and socially withdrawn behavior. Within one to three hours after intravenous administration of TRH or (pyro) glu-his-pro(NH2), 100-1000 mcg. improvement in all areas of psychopathology occurs. The thought processes become more lucid and realistic with an increase in spontaneity of verbal expression. The subjects themselves remark about the sudden clarity of their thinking. Hallucinatory phenomena disappear and the subjects speak with insight about their previously disturbed perceptions. Concomitant changes in affect occur. There is an elevation in mood with a remarkable spontaneity in emotional expression. The subjects show a newly acquired emotional warmth. These beneficial effects continue for a period of several days before gradual regression with a recurrence of schizophrenic symptomatology. However, in no cases to date has the regression been complete.
The improvement in intensity of symptomatology and the "normalization" of personality characteristics make TRH or (pyro) glu-his-pro(NH2) particularly useful agents in the treatment of schizophrenia.
The active ingredients useful in the practice of this invention can be formulated into various pharmaceutical dosage forms such as tablets, capsules, pills, sterile aqueous or nonaqueous solutions for parenteral injection administration, and the like, for immediate or sustained release, by combining one or more of the active compounds with suitable pharmaceutically acceptable carrier or diluents according to methods, well known in the art. Such dosage forms may additionally include excipients, binders, fillers, flavoring and sweetening agents and other therapeutically inert ingredients necessary in the formulation of the desired pharmaceutical preparation.
The following examples are illustrative of suitable dosage formulations useful in the practice of this invention.
EXAMPLE 1
Tablets containing 400 mcg. TRH and having the following composition are prepared according to methods well known in the art.
______________________________________                                    
TRH                 mcg.   400                                            
Starch              mg.    20                                             
Colloidal silica    mg.    4                                              
Magnesium stearate  mg.    1                                              
______________________________________                                    
EXAMPLE 2
Ampoules for intravenous use are prepared containing 200 mcg. of (pyro) glu-his-pro(NH2) in 1 ml. of sterile physiologic saline.
For purposes of the present invention there may be used not only TRH or (pyro) glu-his-pro(NH2) in the treatment of schizophrenia but also the use of congeners and derivatives thereof is contemplated, and such materials are deemed to be the equivalents of the parent materials. It has been shown that certain congeners of TRH, like the parent substance, antagonize the actions of pentobarbital in mice.

Claims (1)

What is claimed is:
1. A method for the treatment of a patient suffering from schizophrenia which comprises the administration to the said patient of a therapeutically effective amount of TRH or L-pyroglutamyl-L-histidyl-L-proline amide.
US05/480,546 1974-06-18 1974-06-18 Method of treating schizophrenia Expired - Lifetime US3932623A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2313075A1 (en) * 1975-04-03 1976-12-31 Takeda Chemical Industries Ltd MEDICINAL PRODUCT BASED ON L-PYROGLUTAMYL-L-HISTIDYL-L-PROLINAMIDE OR ITS SALTS
US4088755A (en) * 1975-05-23 1978-05-09 Takeda Chemical Industries, Ltd. Medicament for remedying schizophrenia
FR2376664A1 (en) * 1977-01-05 1978-08-04 Takeda Chemical Industries Ltd L-PROLINAMIDE DERIVATIVE AND ITS USE AS A THERAPEUTIC MEDIUM FOR THE TREATMENT OF EYE DISEASES
US4146614A (en) * 1976-03-23 1979-03-27 State Of Michigan Threonyl-valyline leucine containing peptides and pharmaceutical compositions
US4608365A (en) * 1984-03-30 1986-08-26 University Of Southern California Treatment of neurologic functions
EP0373904A1 (en) * 1988-12-14 1990-06-20 Massachusetts Institute Of Technology Process and composition for increasing brain dopamine release
US4994467A (en) * 1989-05-31 1991-02-19 Zimmerman Andrew W Treating autism and other developmental disorders in children with NMDA receptor antagonists
US5830866A (en) * 1994-09-12 1998-11-03 The Trustees Of The University Of Pennsylvania Corticotropin release inhibiting factor and methods of using same
EP0979828A1 (en) * 1998-08-04 2000-02-16 Radim S.p.A. A method for the diagnosis of autism
US6039956A (en) * 1994-09-12 2000-03-21 Pennsylvania, Trustees Of The University Of, The Corticotropin release inhibiting factor and methods of using same for treating behavioral symptoms in an anxiety disorder
US6475989B1 (en) * 1997-10-09 2002-11-05 Albert Sattin Use of pyroglutamyl-glutamyl-prolyl amide (EEP) for neurological and neurobehavioral disorders
US20050009753A1 (en) * 1997-10-09 2005-01-13 Albert Sattin Tri-peptides for neurological and neurobehavioral applications
US20050233973A1 (en) * 1997-10-09 2005-10-20 Albert Sattin Tri-peptides for antidepressant applications

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3341412A (en) * 1966-03-04 1967-09-12 Enzomedic Lab Inc Methods of treating schizophrenia

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3341412A (en) * 1966-03-04 1967-09-12 Enzomedic Lab Inc Methods of treating schizophrenia

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Kastin et al.: Lancet, 2, 740 (1972). *
Plotnikoff et al.: Science, 178, 417-418 (1972). *
Prange et al.: Lancet, 2, 999 (1972). *
Sandler et al.: Lancet 1, 612 (1973). *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2313075A1 (en) * 1975-04-03 1976-12-31 Takeda Chemical Industries Ltd MEDICINAL PRODUCT BASED ON L-PYROGLUTAMYL-L-HISTIDYL-L-PROLINAMIDE OR ITS SALTS
US4088755A (en) * 1975-05-23 1978-05-09 Takeda Chemical Industries, Ltd. Medicament for remedying schizophrenia
US4146614A (en) * 1976-03-23 1979-03-27 State Of Michigan Threonyl-valyline leucine containing peptides and pharmaceutical compositions
FR2376664A1 (en) * 1977-01-05 1978-08-04 Takeda Chemical Industries Ltd L-PROLINAMIDE DERIVATIVE AND ITS USE AS A THERAPEUTIC MEDIUM FOR THE TREATMENT OF EYE DISEASES
US4150120A (en) * 1977-01-05 1979-04-17 Takeda Chemical Industries, Ltd. Ophthalmic
US4608365A (en) * 1984-03-30 1986-08-26 University Of Southern California Treatment of neurologic functions
EP0373904A1 (en) * 1988-12-14 1990-06-20 Massachusetts Institute Of Technology Process and composition for increasing brain dopamine release
US4994467A (en) * 1989-05-31 1991-02-19 Zimmerman Andrew W Treating autism and other developmental disorders in children with NMDA receptor antagonists
US5830866A (en) * 1994-09-12 1998-11-03 The Trustees Of The University Of Pennsylvania Corticotropin release inhibiting factor and methods of using same
US6039956A (en) * 1994-09-12 2000-03-21 Pennsylvania, Trustees Of The University Of, The Corticotropin release inhibiting factor and methods of using same for treating behavioral symptoms in an anxiety disorder
US6475989B1 (en) * 1997-10-09 2002-11-05 Albert Sattin Use of pyroglutamyl-glutamyl-prolyl amide (EEP) for neurological and neurobehavioral disorders
US20050009753A1 (en) * 1997-10-09 2005-01-13 Albert Sattin Tri-peptides for neurological and neurobehavioral applications
US20050233973A1 (en) * 1997-10-09 2005-10-20 Albert Sattin Tri-peptides for antidepressant applications
EP0979828A1 (en) * 1998-08-04 2000-02-16 Radim S.p.A. A method for the diagnosis of autism

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